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A Study of LP-300 With Carboplatin and Pemetrexed in Never Smokers With Advanced Lung Adenocarcinoma

NCT05456256

This study is recruiting at 5 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

Summary

The goal of this clinical trial is to determine clinical advantages for LP-300 in combination with carboplatin and pemetrexed in the never smoker patient population. The primary objectives of this study are to determine progression-free survival (PFS) and overall survival (OS) in the study-defined patient population when LP-300 is co-administered with the standard of care chemotherapy drugs carboplatin and pemetrexed compared to carboplatin and pemetrexed alone. This has been designed as a multicenter, open label, phase II trial with 90 patients to be enrolled in the United States.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Adenocarcinoma of Lung
  • Carcinoma, Non-Small-Cell Lung

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
Lantern Pharma Inc.
Last updated on ClinicalTrials.gov
May 4, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 2

  • Precision NextGen Oncology and Research Center · Beverly Hills, CA
  • Los Angeles Cancer Network · Fountain Valley, CA

Pennsylvania · 1

  • Fox Chase Cancer Center · Philadelphia, PA

Texas · 1

  • UT Southwestern Medical Center · Dallas, TX

Virginia · 1

  • Inova Fairfax Hospital · Fairfax, VA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.